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本文引用的文献

1
Clinical Research on Alzheimer's Disease: Progress and Perspectives.阿尔茨海默病的临床研究:进展与展望。
Neurosci Bull. 2018 Dec;34(6):1111-1118. doi: 10.1007/s12264-018-0249-z. Epub 2018 Jun 28.
2
Controversies and Future Directions of Ocular Biomarkers in Alzheimer Disease.阿尔茨海默病眼部生物标志物的争议与未来方向
JAMA Neurol. 2018 Jun 1;75(6):650-651. doi: 10.1001/jamaneurol.2018.0602.
3
Beneficial effects of white wine polyphenols-enriched diet on Alzheimer's disease-like pathology.富含白葡萄酒多酚的饮食对阿尔茨海默病样病理的有益作用。
J Nutr Biochem. 2018 May;55:165-177. doi: 10.1016/j.jnutbio.2018.02.001. Epub 2018 Feb 10.
4
Different doses of folic acid and vitamin B12 to treat rabbits with deep venous thrombosis and hyperhomocysteinemia.不同剂量叶酸和维生素B12治疗兔深静脉血栓形成合并高同型半胱氨酸血症
Exp Ther Med. 2018 Mar;15(3):2874-2878. doi: 10.3892/etm.2018.5751. Epub 2018 Jan 15.
5
Comorbidity Burden of Dementia: A Hospital-Based Retrospective Study from 2003 to 2012 in Seven Cities in China.痴呆的合并症负担:2003 年至 2012 年中国七个城市的医院回顾性研究。
Neurosci Bull. 2017 Dec;33(6):703-710. doi: 10.1007/s12264-017-0193-3. Epub 2017 Nov 13.
6
Retinal amyloid pathology and proof-of-concept imaging trial in Alzheimer's disease.视网膜淀粉样病变与阿尔茨海默病的概念验证成像试验
JCI Insight. 2017 Aug 17;2(16). doi: 10.1172/jci.insight.93621.
7
Ocular indicators of Alzheimer's: exploring disease in the retina.阿尔茨海默病的眼部指标:探索视网膜中的疾病
Acta Neuropathol. 2016 Dec;132(6):767-787. doi: 10.1007/s00401-016-1613-6. Epub 2016 Sep 19.
8
Melanopsin retinal ganglion cell loss in Alzheimer disease.阿尔茨海默病中黑视蛋白视网膜神经节细胞的丧失。
Ann Neurol. 2016 Jan;79(1):90-109. doi: 10.1002/ana.24548. Epub 2015 Dec 18.
9
Neuronal uptake of tau/pS422 antibody and reduced progression of tau pathology in a mouse model of Alzheimer's disease.阿尔茨海默病小鼠模型中神经元对 tau/pS422 抗体的摄取和 tau 病理进展的减少。
Brain. 2014 Oct;137(Pt 10):2834-46. doi: 10.1093/brain/awu213. Epub 2014 Jul 31.
10
Retinal alterations in mild cognitive impairment and Alzheimer's disease: an optical coherence tomography study.轻度认知障碍和阿尔茨海默病中的视网膜改变:一项光学相干断层扫描研究。
J Neurol. 2014 Aug;261(8):1522-30. doi: 10.1007/s00415-014-7374-z. Epub 2014 May 21.

叶酸/维生素 B 可减轻高同型半胱氨酸血症诱导的大鼠视网膜阿尔茨海默病样病变。

Folate/Vitamin B Alleviates Hyperhomocysteinemia-Induced Alzheimer-Like Pathologies in Rat Retina.

机构信息

Department of Pathophysiology, School of Basic Medicine and Collaborative Innovation Center for Brain Science, Key Laboratory for Neurological Disorders of the Ministry of Education of China, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.

Emergency Department, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.

出版信息

Neurosci Bull. 2019 Apr;35(2):325-335. doi: 10.1007/s12264-018-0293-8. Epub 2018 Sep 28.

DOI:10.1007/s12264-018-0293-8
PMID:30264378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6426902/
Abstract

Hyperhomocysteinemia (Hhcy) is an independent risk factor for Alzheimer's disease (AD). Visual dysfunction is commonly found and is positively correlated with the severity of cognitive defects in AD patients. Our previous study demonstrated that Hhcy induces memory deficits with AD-like tau and amyloid-β (Aβ) pathologies in the hippocampus, and supplementation with folate and vitamin B12 (FB) prevents the Hhcy-induced AD-like pathologies in the hippocampus. Here, we investigated whether Hhcy also induces AD-like pathologies in the retina and the effects of FB. An Hhcy rat model was produced by vena caudalis injection of homocysteine for 14 days, and the effects of FB were assessed by simultaneous supplementation with FB in drinking water. We found that Hhcy induced vessel damage with Aβ and tau pathologies in the retina, while simultaneous supplementation with FB remarkably attenuated the Hhcy-induced tau hyperphosphorylation at multiple AD-related sites and Aβ accumulation in the retina. The mechanisms involved downregulation of amyloid precursor protein (APP), presenilin-1, beta-site APP-cleaving enzyme 1, and protein phosphatase-2A. Our data suggest that the retina may serve as a window for evaluating the effects of FB on hyperhomocysteinemia-induced Alzheimer-like pathologies.

摘要

高同型半胱氨酸血症(HHcy)是阿尔茨海默病(AD)的独立危险因素。视觉功能障碍在 AD 患者中很常见,且与认知缺陷的严重程度呈正相关。我们之前的研究表明,HHcy 可导致海马中出现 AD 样 tau 和淀粉样β(Aβ)病理学,并可通过补充叶酸和维生素 B12(FB)预防 HHcy 诱导的海马 AD 样病理学。在这里,我们研究了 HHcy 是否也会在视网膜中诱导 AD 样病理学以及 FB 的作用。通过尾静脉注射同型半胱氨酸 14 天来制备 HHcy 大鼠模型,并通过同时在饮水中补充 FB 来评估 FB 的作用。我们发现 HHcy 可诱导视网膜血管损伤和 Aβ及 tau 病理学,而同时补充 FB 可显著减轻 HHcy 诱导的视网膜中多个 AD 相关位点的 tau 过度磷酸化和 Aβ积累。其机制涉及下调淀粉样前体蛋白(APP)、早老素-1、β位 APP 裂解酶 1 和蛋白磷酸酶-2A。我们的数据表明,视网膜可能作为评估 FB 对 HHcy 诱导的 AD 样病理学作用的窗口。